Assist in initiating, monitoring, and closing clinical trial sites under supervision.
Ensure that clinical trial sites comply with study protocols and regulatory requirements.
Support in maintaining communication with site investigators and coordinators.
Review source documents and case report forms (CRFs) for accuracy and completeness.
Assist in resolving data discrepancies and ensuring data quality.
Maintain essential trial documents (Trial Master File).
Ensure adherence to ICH-GCP, SOPs, and study-specific procedures.
Support preparation of regulatory submissions and ethics committee documents.
Coordinate between sponsors, clinical sites, and internal teams.
Participate in investigator meetings and training sessions.
Job Types: Full-time, Permanent, Fresher
Pay: ₹24,893.05 - ₹42,084.20 per month
Benefits:
Health insurance
Paid sick time
Provident Fund
Work Location: In person
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